A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15748929



Internal ID21391581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21286689..21450688hg38UCSC Ensembl
chr17:21190001..21354000hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38164000
hg19164000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432483
Supporting Variants
SamplesSMI018
Known GenesKCNJ12, KCNJ18, MAP2K3
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15748929
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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